A Case Report of Hereditary Angioedema: Challenges in Diagnosis and Management

Alvina Widhani; Suzy Maria; Rifky Yulian; Anshari Saifuddin Hasibuan; Sukamto Koesnoe

A Case Report of Hereditary Angioedema: Challenges in Diagnosis and Management

Alvina Widhani, Suzy Maria, Rifky Yulian, Anshari Saifuddin Hasibuan, Sukamto Koesnoe

Department of Internal Medicine

Research output: Contribution to journal › Article › peer-review

Abstract

Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder which causes bradykinin mediated angioedema. Although it can be life threatening, HAE may be underdiagnosed due to a lack of awareness of the disease and limited access to laboratory testing. Here, we report a case of HAE which was diagnosed only after the patient was referred for COVID-19 vaccination even though he had been experiencing recurrent angioedema for the past 30 years.

Original language	English
Pages (from-to)	205-210
Number of pages	6
Journal	Acta medica Indonesiana
Volume	55
Issue number	2
Publication status	Published - 2023

Keywords

angioedema
diagnosis
Hereditary
management

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Cite this

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abstract = "Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder which causes bradykinin mediated angioedema. Although it can be life threatening, HAE may be underdiagnosed due to a lack of awareness of the disease and limited access to laboratory testing. Here, we report a case of HAE which was diagnosed only after the patient was referred for COVID-19 vaccination even though he had been experiencing recurrent angioedema for the past 30 years.",

keywords = "angioedema, diagnosis, Hereditary, management",

author = "Alvina Widhani and Suzy Maria and Rifky Yulian and Hasibuan, {Anshari Saifuddin} and Sukamto Koesnoe",

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language = "English",

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issn = "0125-9326",

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TY - JOUR

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T2 - Challenges in Diagnosis and Management

AU - Widhani, Alvina

AU - Maria, Suzy

AU - Yulian, Rifky

AU - Hasibuan, Anshari Saifuddin

AU - Koesnoe, Sukamto

PY - 2023

Y1 - 2023

N2 - Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder which causes bradykinin mediated angioedema. Although it can be life threatening, HAE may be underdiagnosed due to a lack of awareness of the disease and limited access to laboratory testing. Here, we report a case of HAE which was diagnosed only after the patient was referred for COVID-19 vaccination even though he had been experiencing recurrent angioedema for the past 30 years.

AB - Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder which causes bradykinin mediated angioedema. Although it can be life threatening, HAE may be underdiagnosed due to a lack of awareness of the disease and limited access to laboratory testing. Here, we report a case of HAE which was diagnosed only after the patient was referred for COVID-19 vaccination even though he had been experiencing recurrent angioedema for the past 30 years.

KW - angioedema

KW - diagnosis

KW - Hereditary

KW - management

UR - http://www.scopus.com/inward/record.url?scp=85166394139&partnerID=8YFLogxK

M3 - Article

C2 - 37524594

AN - SCOPUS:85166394139

SN - 0125-9326

VL - 55

SP - 205

EP - 210

JO - Acta medica Indonesiana

JF - Acta medica Indonesiana

IS - 2

ER -

A Case Report of Hereditary Angioedema: Challenges in Diagnosis and Management

Abstract

Keywords

UN SDGs

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